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Select item 74415591.

rs7441559 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 4:68546227 (GRCh38)
4:69411945 (GRCh37)
Canonical SPDI:: NC_000004.12:68546226:T:A,NC_000004.12:68546226:T:G
Gene:: UGT2B17 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.082617/980 (ALFA)
T=0./0 (Siberian)
T=0.00501/5 (GoNL)
T=0.018797/10 (NorthernSweden)
T=0.021277/4 (Qatari)
T=0.024845/8 (SGDP_PRJ)
T=0.05/2 (GENOME_DK)
T=0.103086/12019 (GnomAD)
T=0.196752/985 (1000Genomes)
T=0.294523/1156 (TOMMO)
T=0.300231/260 (KOREAN)
T=0.349593/172 (Korea1K)
HGVS:: NC_000004.12:g.68546227T>A, NC_000004.12:g.68546227T>G, NC_000004.11:g.69411945T>A, NC_000004.11:g.69411945T>G, NG_017033.1:g.27301A>T, NG_017033.1:g.27301A>C

Supplemental Content

dbSNP